Method of predicting a predisposition to qt prolongation

ABSTRACT

The present invention describes an association between genetic polymorphisms in the FAM13A1 (family with sequence similarity 13, member A1) gene and a predisposition to prolongation of the QT interval, and provides related methods for the prediction of such a predisposition, the administration of QT interval-prolonging compounds to individuals having such a predisposition, and determining whether a compound is capable of inducing QT prolongation.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of co-pending U.S. application Ser. No. 13/263,075, filed Oct. 5, 2011, which is a US National Stage application under 35 USC 371 of PCT/US2010/029931, filed Apr. 5, 2010, which claims the benefit of U.S. Provisional Patent Application No. 61/167,138, filed Apr. 6, 2009, each of which is incorporated herein as though fully set forth.

BACKGROUND OF THE INVENTION

1. Technical Field

The invention relates generally to a method of predicting an individual's predisposition to QT prolongation, and more particularly, to a method of predicting such predisposition based on a sequence of the individual's FAM13A1 (family with sequence similarity 13, member A1) gene.

2. Background

Prolongation of the electrocardiographic QT interval (the time between the start of the Q wave and the end of the T wave) is referred to as long QT syndrome (LQTS). LQTS may comprise a genetic component. In some patients with LQTS, QT prolongation can be a chronic condition. In some persons, LQTS may be induced by the administration of an active pharmaceutical ingredient that prolongs the QT interval. A number of compounds are believed to be capable of prolonging the QT interval. These include amiodarone, arsenic trioxide, bepridil, chloroquine, chlorpromazine, cisapride, clarithromycin, disopyramide, dofetilide, domperidone, droperidol, erythromycin, halofantrine, haloperidol, ibutilide, iloperidone, levomethadyl, mesoridazine, methadone, pentamidine, pimozide, procainamide, quinidine, sotalol, sparfloxacin, and thioridazine.

Other compounds are suspected of being capable of prolonging the QT interval, although such prolongation has not been definitively established. These include alfuzosin, amantadine, azithromycin, chloral hydrate, clozapine, dolasetron, felbamate, flecainide, foscarnet, fosphenytoin, gatifloxacin, gemifloxacin, granisetron, indapamide, isradipine, levofloxacin, lithium, moexipril, moxifloxacin, nicardipine, octreotide, ofloxacin, ondansetron, quetiapine, ranolazine, risperidone, roxithromycin, tacrolimus, tamoxifen, telithromycin, tizanidine, vardenafil, venlafaxine, voriconazole, and ziprasidone.

Individuals at risk of suffering LQTS are advised not to use still other compounds, due to the possibility that they may prolong the QT interval. These include albuterol, amitriptyline, amoxapine, amphetamine, dextroamphetamine, atomoxetine, chloroquine, ciprofloxacin, citalopram, clomipramine, cocaine, desipramine, dexmethylphenidate, dobutamine, dopamine, doxepin, ephedrine, epinephrine, fenfluramine, fluconazole, fluoxetine, galantamine, imipramine, isoproterenol, itraconazole, ketoconazole, levalbuterol, metaproterenol, methylphenidate, mexiletine, midodrine, norepinephrine, nortriptyline, paroxetine, phentermine, phenylephrine, phenylpropanolamine, protriptyline, pseudoephedrine, ritodrine, salmeterol, sertraline, sibutramine, solifenacin, terbutaline, tolterodine, trimethoprim-sulfa, and trimipramine.

The FAM13A1 gene has been mapped by Cohen et al. to 4q22.1 and determined to contain 18 exons. Cohen et al., Cloning and characterization of FAM13A1—a gene near a milk protein QTL on BTA6: evidence for population-wide linkage disequilibrium in Israeli Holsteins, Genomics 2004 August; 84(2):374-83 PubMed ID: 15234000. Cohen et al. cloned the first member of a novel gene family (FAM13) in bovine. This gene is neighboring an extracellular matrix (ECM) cluster. This cluster of genes containing sequence motifs essential for integrin-receptor interactions is located on HSA4q21 and on BTA6, within the critical region of a quantitative trait locus (QTL) affecting milk protein production. Genes within this cluster are involved in the formation of bone and lobuloalveolar structures in mammary gland and in kidney function.

SUMMARY OF THE INVENTION

The present invention describes an association between genetic polymorphisms in the FAM13A1 (family with sequence similarity 13, member A1) gene and a predisposition to prolongation of the QT interval, and provides related methods for the diagnosis of such predisposition and for the administration of QT interval-prolonging compounds to individuals having such a predisposition.

A first aspect of the invention provides a method of administering to an individual a compound capable of prolonging the individual's QT interval, the method comprising determining at least a portion of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene sequence; and in the case that a portion of the individual's FAM13A1 sequence is associated with an increased risk of QT prolongation, administering to the individual a quantity of the compound less than would be administered to an individual having a FAM13A1 gene sequence not associated with an increased risk of QT prolongation, or electing instead to treat the individual with a different compound not known to be associated with QT prolongation.

A second aspect of the invention provides a method of determining whether or not an individual is predisposed to prolongation of the QT interval, the method comprising: determining at least a portion of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene sequence.

A third aspect of the invention provides a method of administering a compound capable of prolonging a QT interval to an individual suffering from long QT syndrome (LQTS), the method comprising: determining at least a portion of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene sequence; and administering to the individual a quantity of the compound based on the individual's FAM13A1 gene sequence.

A fourth aspect of the invention provides a method of administering to an individual a compound capable of prolonging the individual's QT interval, the method comprising: characterizing an expression product of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene; and in the case that the characterized expression product is associated with an increased risk of QT prolongation, administering to the individual a quantity of the compound less than would be administered to an individual having an expression product not associated with an increased risk of QT prolongation. Expression products of the FAM13A1 gene may include, for example, mRNA and protein including any isoform of the mRNA and protein.

A fifth aspect of the invention provides a method of determining whether an individual is predisposed to prolongation of the QT interval, the method comprising: characterizing an expression product of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene.

A sixth aspect of the invention provides a method of administering a compound capable of prolonging a QT interval to an individual suffering from long QT syndrome (LQTS), the method comprising: characterizing an expression product of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene; and administering to the individual a quantity of the compound based on the characterized expression product.

A seventh aspect of the invention provides a method of determining whether a compound is capable of prolonging QT interval in an individual, the method comprising: measuring an expression product of the individual's FAM13A1 (family with sequence similarity 13, member A1) gene; administering to the individual a quantity of the compound; remeasuring the expression product of the individual's FAM13A1 gene; and determining whether the compound is capable of prolonging the individual's QT interval based on a difference in the measurements of the expression product of the individual's FAM13A1 gene.

An eighth aspect of the invention provides a method of determining whether a compound is capable of prolonging a QT interval in an individual, the method comprising: measuring a QT interval of each of a plurality of test organisms, the plurality including a first test organism having a FAM13A1 (family with sequence similarity 13, member A1) genotype associated with a predisposition for prolongation of QT interval and a second organism having FAM13A1 genotype not associated with a predisposition for prolongation of QT interval; administering a quantity of the compound to each of the plurality of test organisms; remeasuring a QT interval of at least the first test organism; and determining that the compound is capable of prolonging a QT interval in an individual in the case that the remeasured QT interval is greater than the measured QT interval. Test organisms may include, for example, humans, animal models, and/or cell lines.

DETAILED DESCRIPTION OF THE INVENTION

As indicated above, the invention provides a method of predicting an individual's predisposition to QT prolongation based on the sequence of the individual's FAM13A1 (family with sequence similarity 13, member A1) gene.

At least one single nucleotide polymorphisms (SNPs) within the FAM13A1 gene has been found to have a significant correlation to a predisposition to drug-induced QT prolongation. Table 1, below, shows such SNPs and the genotypes associated with QT prolongation following the administration of iloperidone.

TABLE 1 FAM13A1 SNP Genotypes and QT Prolongation Following Administration of lloperidone Lowest Affymetrix SNP QTc Allele No. rs_number¹ Position² change P value³ A Allele B SNP_A-4194821 rs2924941 89863220 AA 0.809963782 C T SNP_A-2093666 rs3017895 89868514 BB 0.530500186 C T SNP_A-1977994 rs17014483 89886614 non-BB 0.128385989 C T SNP_A-2306584 rs7683339 89891505 AB 0.090492451 C T SNP_A-2162316 rs6841084 89914508 AB 0.507117232 A T SNP_A-4296194 rs12507401 89915913 non-AA 0.064868339 C G SNP_A-4283738 rs17014546 89916235 AA 0.018465115 C T SNP_A-1943446 rs17014602 89950009 non-AA 0.257980315 C G SNP_A-2065917 rs4544678 89950302 AA 0.035706045 A G SNP_A-1808669 rs7691186 89950932 AA 0.039030668 A G SNP_A-2067635 rs6814344 89952905 BB 0.018558356 C T SNP_A-2251180 rs13131633 89958502 BB 0.022420846 A G SNP_A-1906173 rs3775378 89959101 non-BB 1.58682E-07 C T SNP_A-2200417 rs2305934 89963265 BB 0.048871501 A G SNP_A-4243899 rs9991039 89984895 AA 0.869452703 A T SNP_A-4290819 rs17014687 89985586 non-BB 0.010624243 C T SNP_A-1870378 rs1379932 90019915 AA 0.310046334 C T SNP_A-2200089 rs1458551 90031265 AA 0.437083654 C T SNP_A-4287986 rs2609265 90045989 nonAB 0.05605724 C T SNP_A-4291320 rs2609264 90047103 nonAB 0.040104616 C T SNP_A-2284008 rs2609261 90054508 BB 0.198209042 A G SNP_A-2152738 rs1458553 90055014 nonAA 0.32632219 A G SNP_A-2190887 rs2609260 90055842 nonAB 0.660268059 A G SNP_A-1824897 rs10008568 90073215 nonAB 0.073628051 A G SNP_A-2094935 rs2464526 90098686 AA 0.148471845 A G SNP_A-4284617 rs2904259 90104737 AA 0.085423976 C T SNP_A-1830961 rs2609266 90106817 AA 0.124904291 C T SNP_A-1977995 rs1921679 90109807 AA 0.124831097 A G SNP_A-4264355 rs2178583 90110165 AA 0.275411131 A T SNP_A-1977996 rs2178584 90110221 BB 0.162876336 C T SNP_A-2032491 rs10033484 90124495 AA 0.216398627 A G SNP_A-1832183 rs7697075 90127331 AA 0.196280013 A G ¹Official SNP nomenclature according to NCBI db SNP version 126, May 2006. ²Chromosomal position based on the NCBI Build 36.1, March 2006. ³P value of genotype having highest QT values versus all other genotypes.

A genotype of TT at the rs3775378 locus was found to most accurately predict a predisposition to QT prolongation. This genotype is included amongst all genotypes associated with a predisposition to QT prolongation. Therefore, individuals having a genotype of TT at the rs3775378 locus may be considered predisposed to QT prolongation following the administration of a compound capable of prolonging the QT interval.

Since the QT interval changes with changes in heart rate, the QT interval is often measured as a corrected QT (QTc) interval. Any number of formulas may be employed to calculate the QTc, including, for example, the Fridericia formula (QTcF), the Bazett formula (QTcB), and the Rautaharju formula (QTp), among others. In the studies described herein, QT was calculated using the Fridericia formula. However, the present invention includes the use of any such formula or method for calculating a QTc or an uncorrected QT.

As noted above, a large number of compounds are known or suspected to be capable of inducing QT prolongation in some individuals, including individuals not suffering from LQTS. One such compound is iloperidone. Iloperidone is disclosed in U.S. Pat. Nos. 5,364,866, 5,658,911, and 6,140,345, each of which is incorporated herein by reference. Metabolites of iloperidone may also be capable of prolonging a QT interval. Metabolites of Iloperidone, e.g., 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanol, are described in International Patent Application Publication No. WO03020707, which is also incorporated herein by reference.

Other iloperidone metabolites include: 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-hydroxyphenyl]ethanone; 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]-2-hydroxyethanone; 4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-hydroxy-α-methylbenzene methanol; 4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxyl-2-hydroxy-5-methoxy-α-methylbenzenemethanol; 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-2-hydroxy-5-methoxyphenyl]ethanone; and 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-2,5-dihydroxyphenyl]ethanone. See U.S. Pat. No. 5,364,866 and International Patent Application Publication Nos. WO9309276 and WO9511680, which are incorporated herein by reference.

Using the genotypes at the SNP loci above, it is possible, with a high degree of certainty, to predict an individual's predisposition to QT prolongation. Table 2 below shows the results of a study of 174 individuals, each of whom was genotyped at the rs3775378 locus and their QT interval measured following the oral administration of 24 mg/day B.I.D. of iloperidone for a period of two weeks.

TABLE 2 QT Prolongation and Presence or Absence of a Genotype for SNP_A- 1906173, rs3775378 Associated with a Predisposition to QT Prolongation Change negative positive Threshold Low QT High QT Odds predictive predictive (msec) − test + test − test + test Ratio p value sensitivity specificity value value QT > 5 63 0 101 9 0.9741 0.08 1.00 0.38 1.00 QT > 15 105 1 59 8 14.24 0.0133 0.12 0.99 0.64 0.89 QT > 30 142 3 22 6 12.91 0.0006 0.21 0.98 0.87 0.67

As can be seen in Table 2, an individual's FAM13A1 sequence at the SNP_A-1906173, rs3775378 locus is highly predictive of whether the individual will experience QT prolongation following the administration of iloperidone. For example, using the lowest threshold of a change in QTc interval (between baseline and the end of the second week) greater than 5 milliseconds (normal QTc intervals are between 0.30 and 0.44 seconds for males and between 0.30 and 0.45 for females), 9 of those individuals with the TT genotype (test is considered positive if the genotype for SNP_A-1906173, rs3775378 is TT) experienced QT prolongation while no such individuals did not. The resulting sensitivity (probability that the individual will have a SNP genotype associated with a predisposition to QT prolongation, given that he/she experienced QT prolongation) of 0.08, specificity (probability that the individual will not have a SNP genotype associated with a predisposition to QT prolongation, given that he/she did not experience QT prolongation) of 1.0, negative predictive value (probability that the individual will not experience QT prolongation, given that he/she does not have a SNP genotype associated with a predisposition to QT prolongation) of 0.38, and a positive predictive value (probability that the individual will experience QT prolongation, given that he/she has a SNP genotype associated with a predisposition to QT prolongation) of 1.0, permit one to predict with great accuracy that an individual possessing the TT genotype is likely to experience QT prolongation.

The use of higher thresholds (i.e., QTs greater than 15 and 30 milliseconds) yielded markedly increased negative predictive values (0.64 and 0.87, respectively). The associated decrease in positive predictive values, from 1.0 for QTs greater than 5 milliseconds to 0.67 for QTs greater than 30 milliseconds) suggests that additional factors affect more severe QT prolongation.

As the data in Table 2 show, an individual's FAM13A1 sequence at the SNP loci above may be used to predict whether an individual is predisposed to QT prolongation due to the administration of a compound capable of prolonging the QT interval. That is, individuals having a genotype of TT at the rs3775378 locus may reliably be predicted to experience a prolonged QT interval (i.e., a change in QT interval of at least 5 milliseconds) following the administration of a compound capable of prolonging the QT interval. Similarly, individuals having a genotype other than TT at the rs3775378 locus may reliably be predicted to not experience severe QT prolongation (i.e., a change in QT interval of greater than 15 milliseconds) following the administration of a compound capable of prolonging the QT interval.

The ability to make such predictions may be used in deciding whether to treat an individual with a particular compound and/or in determining the dosage appropriate for the individual. For example, an individual predicted to experience QT prolongation may be treated with an alternative compound not known or suspected to cause QT prolongation or may be administered a lower dose of a compound capable of causing QT prolongation than would be administered to an individual not predicted to experience QT prolongation.

The present invention also includes the administration of another compound useful in treating LQTS, in addition to one or more of the compounds above. Compounds useful in treating LQTS and/or preventing cardiac events resulting from LQTS, include, for example, beta blockers, such as propranolol, nadolol, atenolol, metoprolol.

The present invention also includes the prediction of an individual's predisposition for QT prolongation based on one or more of the SNP loci above in combination with the individual's genotype or gene sequence at one or more additional genes or loci. For example, International Patent Application Publication No. WO2006039663, incorporated herein by reference, describes a method of treating an individual with a compound capable of inducing QT prolongation based on the individual's CYP2D6 genotype. Other genotypes and/or gene sequences may similarly be used in combination with the SNP loci above, including those associated with LQTS. It should also be understood that the present invention includes the characterization of an expression product of the FAM13A1 gene rather than, or in addition to, the determination of one or more SNP genotypes within the FAM13A1 gene. For example, by determining a sequence of an mRNA strand transcribed from the FAM13A1 gene, it is possible to determine the sequence of the FAM13A1 gene itself and, as described above, determine whether the FAM13A1 gene sequence is associated with a predisposition to QT prolongation.

Similarly, by properly characterizing a functional peptide or protein, including the FAM13A1 enzyme, translated from the mRNA strand above, it is possible to determine the sequence of the FAM13A1 gene itself and, as described above, determine whether the FAM13A1 gene sequence is associated with a predisposition to QT prolongation. In addition, the present invention includes determining whether a compound is capable of prolonging a QT interval in an individual. This may be done, for example, by measuring a change in QT interval in a test organism (e.g., human, animal model, cell line) known to possess a FAM13A1 genotype associated with a predisposition to QT prolongation following the administration of a quantity of compound under study.

Preferably, the compound is also administered to a test organism known to possess a FAM13A1 genotype not associated with a predisposition to QT prolongation.

The foregoing description of various aspects of the invention has been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise form disclosed, and obviously, many modifications and variations are possible. Such modifications and variations that may be apparent to a person skilled in the art are intended to be included within the scope of the invention as defined by the accompanying claims. 

1. A method of administering to an individual a compound capable of prolonging the individual's QT interval, the method comprising: determining at least a portion of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene sequence; and in the case that a portion of the individual's FAM13A1 gene sequence is associated with an increased risk of QT prolongation, administering to the individual a quantity of the compound less than would be administered to an individual having a FAM13A1 gene sequence not associated with an increased risk of QT prolongation.
 2. The method of claim 1, wherein determining includes determining the individual's genotype at the rs3775378 locus, and wherein the genotype associated with an increased risk of QT prolongation is TT.
 3. (canceled)
 4. The method of claim 1, further comprising: determining the individual's CYP2D6 genotype.
 5. The method of claim 1, wherein the compound is selected from a group consisting of: amiodarone, arsenic trioxide, bepridil, chloroquine, chlorpromazine, cisapride, clarithromycin, disopyramide, dofetilide, domperidone, droperidol, erythromycin, halofantrine, haloperidol, ibutilide, iloperidone, levomethadyl, mesoridazine, methadone, pentamidine, pimozide, procainamide, quinidine, sotalol, sparfloxacin, thioridazine; alfuzosin, amantadine, azithromycin, chloral hydrate, clozapine, dolasetron, felbamate, flecainide, foscarnet, fosphenytoin, gatifloxacin, gemifloxacin, granisetron, indapamide, isradipine, levofloxacin, lithium, moexipril, moxifloxacin, nicardipine, octreotide, ofloxacin, ondansetron, quetiapine, ranolazine, risperidone, roxithromycin, tacrolimus, tamoxifen, telithromycin, tizanidine, vardenafil, venlafaxine, voriconazole, ziprasidone; albuterol, amitriptyline, amoxapine, amphetamine, dextroamphetamine, atomoxetine, chloroquine, ciprofloxacin, citalopram, clomipramine, cocaine, desipramine, dexmethylphenidate, dobutamine, dopamine, doxepin, ephedrine, epinephrine, fenfluramine, fluconazole, fluoxetine, galantamine, imipramine, isoproterenol, itraconazole, ketoconazole, levalbuterol, metaproterenol, methylphenidate, mexiletine, midodrine, norepinephrine, nortriptyline, paroxetine, phentermine, phenylephrine, phenylpropanolamine, protriptyline, pseudoephedrine, ritodrine, salmeterol, sertraline, sibutramine, solifenacin, terbutaline, tolterodine, trimethoprim-sulfa, trimipramine, and metabolites, pharmaceutically-acceptable salts, and combinations thereof.
 6. The method of claim 5, wherein the compound has the formula:

wherein: R is, independently, hydrogen, lower alkyl, lower alkoxy, hydroxyl, carboxyl, lower hydroxyketone, lower alkanol, hydroxyl acetic acid, pyruvic acid, ethanediol, chlorine, fluorine, bromine, iodine, amino, lower mono or dialkylamino, nitro, lower alkyl thio, trifluoromethoxy, cyano, acylamino, trifluoromethyl, trifluoroacetyl, aminocarbonyl, monoaklylaminocarbonyl, dialkylaminocarbonyl, formyl,

alkyl is lower alkyl, branched or straight and saturated or unsaturated; acyl is lower alkyl or lower alkyloxy bonded through a carbonyl; aryl is phenyl or phenyl substituted with at least one group, R₅, wherein each R₅ is, independently, hydrogen, lower alkyl, lower alkoxy, hydroxy, chlorine, fluorine, bromine, iodine, lower monoalkylamino, lower dialkylamino, nitro, cyano, trifluoromethyl, or trifluoromethoxy; heteroaryl is is a five- or six-membered aryl ring having at least one heteroatom, Q₃, wherein each Q₃ is, independently, —O—, —S—, —N(H)—, or —C(H)═N—W is CH₂ or CHR₈ or N—R₉; R₁ is —H, lower alkyl, —OH, halo, lower alkoxy, trifluormethyl, nitro, or amino; R₂ is C₂-C₅ alkylene, alkenylene (cis or trans), or alkynylene, optionally substituted by at least one C₁-C₆ linear alkyl group, phenyl group or

where Z₁ is lower alkyl, —OH, lower alkoxy, —CF₃, —NO₂, —NH₂, or halogen; R₃ is lower alkyl or hydrogen; R₇ is hydrogen, lower alkyl, or acyl; R₈ is lower alkyl; R₉ is hydroxy, lower alkoxy, or —NHR₁₀; R₁₀ is hydrogen, lower alkyl, C₁-C₃ acyl, aryl,

X₁, X₂, and X₃ are, independently, —O—, —S—, ═N—, or —N(R₃)—, or X₁ and X₂ are not covalently bound to each other and are, independently, —OH, ═O, —R₃, or ═NR₃; lower is 1-4 carbon atoms; m is 1, 2, or 3; and n is 1 or
 2. 7. The method of claim 6, wherein: R is —C(O)CH₂OH, —CH(OH)C(O)CH₂OH, —C(O)OH, CH(OH)CH₃, or C(O)CH₃; R₁ is halo; X₁ and X₂ are different and are ═O, —OH, ═N—, or —O—; R₂ is C₂-C₄ alkylene or alkenylene; R₃ is hydrogen, methyl, or ethyl; X₃ is —O—; R is


8. The method of claim 7, wherein the compound of Formula 1 is 1-[4-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone, as shown in Formula 1B:


9. The method of claim 7, wherein the compound of Formula 1 is 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanol, as shown in Formula 1C:


10. A method of determining whether an individual is predisposed to prolongation of the QT interval, the method comprising: determining at least a portion of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene sequence.
 11. The method of claim 10, further comprising: in the case that a portion of the individual's FAM13A1 gene sequence is associated with an increased risk of QT prolongation, administering to the individual a compound not known or suspected to cause QT prolongation.
 12. The method of claim 10, wherein determining includes determining the individual's genotype at the rs3775378 locus, and wherein the genotype associated with an increased risk of QT prolongation is TT.
 13. (canceled)
 14. The method of claim 10, further comprising: determining the individual's CYP2D6 genotype.
 15. A method of administering a compound capable of prolonging a QT interval to an individual suffering from long QT syndrome (LQTS), the method comprising: determining at least a portion of an individual's FAM13A1 (family with sequence similarity 13, member A1) gene sequence; and administering to the individual a quantity of the compound based on the individual's FAM13A1 gene sequence.
 16. The method of claim 15, wherein determining includes determining the individual's genotype at the rs3775378 locus, and wherein the genotype associated with an increased risk of QT prolongation is TT.
 17. (canceled)
 18. The method of claim 15, further comprising: determining the individual's CYP2D6 genotype.
 19. The method of claim 15, wherein the compound is selected from a group consisting of: amiodarone, arsenic trioxide, bepridil, chloroquine, chlorpromazine, cisapride, clarithromycin, disopyramide, dofetilide, domperidone, droperidol, erythromycin, halofantrine, haloperidol, ibutilide, iloperidone, levomethadyl, mesoridazine, methadone, pentamidine, pimozide, procainamide, quinidine, sotalol, sparfloxacin, thioridazine; alfuzosin, amantadine, azithromycin, chloral hydrate, clozapine, dolasetron, felbamate, flecainide, foscarnet, fosphenytoin, gatifloxacin, gemifloxacin, granisetron, indapamide, isradipine, levofloxacin, lithium, moexipril, moxifloxacin, nicardipine, octreotide, ofloxacin, ondansetron, quetiapine, ranolazine, risperidone, roxithromycin, tacrolimus, tamoxifen, telithromycin, tizanidine, vardenafil, venlafaxine, voriconazole, ziprasidone; albuterol, amitriptyline, amoxapine, amphetamine, dextroamphetamine, atomoxetine, chloroquine, ciprofloxacin, citalopram, clomipramine, cocaine, desipramine, dexmethylphenidate, dobutamine, dopamine, doxepin, ephedrine, epinephrine, fenfluramine, fluconazole, fluoxetine, galantamine, imipramine, isoproterenol, itraconazole, ketoconazole, levalbuterol, metaproterenol, methylphenidate, mexiletine, midodrine, norepinephrine, nortriptyline, paroxetine, phentermine, phenylephrine, phenylpropanolamine, protriptyline, pseudoephedrine, ritodrine, salmeterol, sertraline, sibutramine, solifenacin, terbutaline, tolterodine, trimethoprim-sulfa, trimipramine, and metabolites, pharmaceutically-acceptable salts, and combinations thereof.
 20. The method of claim 19, wherein the compound has the formula:

wherein: R is, independently, hydrogen, lower alkyl, lower alkoxy, hydroxyl, carboxyl, lower hydroxyketone, lower alkanol, hydroxyl acetic acid, pyruvic acid, ethanediol, chlorine, fluorine, bromine, iodine, amino, lower mono or dialkylamino, nitro, lower alkyl thio, trifluoromethoxy, cyano, acylamino, trifluoromethyl, trifluoroacetyl, aminocarbonyl, monoaklylaminocarbonyl, dialkylaminocarbonyl, formyl,

alkyl is lower alkyl, branched or straight and saturated or unsaturated; acyl is lower alkyl or lower alkyloxy bonded through a carbonyl; aryl is phenyl or phenyl substituted with at least one group, R₅, wherein each R₅ is, independently, hydrogen, lower alkyl, lower alkoxy, hydroxy, chlorine, fluorine, bromine, iodine, lower monoalkylamino, lower dialkylamino, nitro, cyano, trifluoromethyl, or trifluoromethoxy; heteroaryl is is a five- or six-membered aryl ring having at least one heteroatom, Q₃, wherein each Q₃ is, independently, —O—, —S—, —N(H)—, or —C(H)═N—W is CH₂ or CHR₈ or N—R₉; R₁ is —H, lower alkyl, —OH, halo, lower alkoxy, trifluormethyl, nitro, or amino; R₂ is C₂-C₅ alkylene, alkenylene (cis or trans), or alkynylene, optionally substituted by at least one C₁-C₆ linear alkyl group, phenyl group or

where Z₁ is lower alkyl, —OH, lower alkoxy, —CF₃, —NO₂, —NH₂, or halogen; R₃ is lower alkyl or hydrogen; R₇ is hydrogen, lower alkyl, or acyl; R₈ is lower alkyl; R₉ is hydroxy, lower alkoxy, or —NHR₁₀; R₁₀ is hydrogen, lower alkyl, C₁-C₃ acyl, aryl,

X₁, X₂, and X₃ are, independently, —O—, —S—, ═N—, or —N(R₃)—, or X₁ and X₂ are not covalently bound to each other and are, independently, —OH, ═O, —R₃, or ═NR₃; lower is 1-4 carbon atoms; m is 1, 2, or 3; and n is 1 or
 2. 21. The method of claim 20, wherein: R is —C(O)CH₂OH, —CH(OH)C(O)CH₂OH, —C(O)OH, CH(OH)CH₃, or C(O)CH₃; R₁ is halo; X₁ and X₂ are different and are ═O, —OH, ═N—, or —O—; R₂ is C₂-C₄ alkylene or alkenylene; R₃ is hydrogen, methyl, or ethyl; X₃ is —O—; R is


22. The method of claim 21, wherein the compound of Formula 1 is 1-[4-3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone, as shown in Formula 1B:


23. The method of claim 21, wherein the compound of Formula 1 is 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanol, as shown in Formula 1C:

24-33. (canceled) 